RALYL
RALY RNA binding protein like
Summary
Enables identical protein binding activity. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs773385570 | 8:85,097,242 | A/C | — | uncertain significance |
| rs146723787 | 8:85,122,163 | G/A | intron variant | — |
| rs562378797 | 8:85,215,405 | T/C | — | — |
| rs200973667 | 8:85,441,663 | T/C | — | uncertain significance |
| rs28465008 | 8:85,523,756 | C/T | intron variant | — |
| rs7842614 | 8:85,526,604 | A/G | intron variant | — |
| rs13266372 | 8:85,626,666 | G/T | intron variant | — |
| rs2492424750 | 8:85,686,869 | G/C | — | uncertain significance |
| rs191234927 | 8:85,737,571 | A/G | regulatory region variant | — |
| rs1380511935 | 8:85,762,228 | G/T | — | uncertain significance |
| rs2135058856 | 8:85,774,548 | G/T | — | uncertain significance |
| rs2494837444 | 8:85,774,559 | C/G | — | uncertain significance |
| rs527942610 | 8:85,774,568 | C/T | — | uncertain significance |
| rs766785304 | 8:85,774,569 | G/A | — | uncertain significance |
| rs147345564 | 8:85,774,617 | G/A | — | uncertain significance |
| rs2494846626 | 8:85,774,642 | G/A | — | uncertain significance |
| rs2494847260 | 8:85,774,652 | T/A | — | uncertain significance |
| rs751482365 | 8:85,785,546 | A/G | — | uncertain significance |
| rs772399055 | 8:85,785,593 | C/T | — | uncertain significance |
| rs376378537 | 8:85,785,594 | G/T | — | uncertain significance |
| rs771106775 | 8:85,799,845 | A/G | — | uncertain significance |
| rs772217937 | 8:85,799,865 | A/G | — | uncertain significance |
| rs750010621 | 8:85,799,890 | G/A | — | uncertain significance |
| rs2495709351 | 8:85,799,911 | A/C | — | uncertain significance |
| rs371413262 | 8:85,799,914 | C/T | missense variant | — |
| rs766059077 | 8:85,799,988 | G/A | — | uncertain significance |
| rs1388216492 | 8:85,799,996 | T/A | — | uncertain significance |
| rs7002227 | 8:85,800,743 | A/G | intron variant | — |
| rs965502531 | 8:85,833,130 | T/G | — | uncertain significance |
| rs1299047439 | 8:85,833,138 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.